• 图片1

cembrene A

  • CasNo:31570-39-5

Product Description

Manufacturer Supply Best Quality cembrene A 31570-39-5 with Efficient Transportation

  • Molecular Formula: C20H32
  • Molecular Weight: 272.474
  • Vapor Pressure: 2.48E-05mmHg at 25°C 
  • Refractive Index: nD30 1.5102 
  • Boiling Point: 369.7°Cat760mmHg 
  • Flash Point: 169°C 
  • PSA: 0.00000 
  • Density: 0.831g/cm3 
  • LogP: 6.76190 

cembrene A(Cas 31570-39-5) Usage

Definition

ChEBI: A fourteen-membered macrocyclic diterpene consisting of 1,5,9-trimethyl-12-(prop-1-en-2-yl)cyclotetradecane having three endocyclic double bonds located at positions 1, 5 and 9.

InChI:InChI=1/C20H32/c1-16(2)20-14-12-18(4)10-6-8-17(3)9-7-11-19(5)13-15-20/h8,11-12,20H,1,6-7,9-10,13-15H2,2-5H3/b17-8+,18-12+,19-11+/t20-/m0/s1

31570-39-5 Relevant articles

Mechanistic investigations on multiproduct β-himachalene synthase from Cryptosporangium arvum

Rinkel, Jan,Dickschat, Jeroen S.

supporting information, p. 1008 - 1019 (2019/06/08)

A bacterial terpene synthase from Crypto...

Studies on macrocyclic diterpenoids (XVII): Total synthesis of (-)-cembrene-A and (+)-3,4-epoxycembrene-A by titanium-induced carbonyl coupling reactions

Yue, Xiangjun,Li, Yulin

, p. 736 - 740 (2007/10/03)

Efficient total syntheses of (R)-cembren...

Novel Synthesis of (-)-(R)-Cembrene A, Synthesis of (+)-(R)-Cembrenene and (+)-(S)-Cembrene

Farkas, Imre,Pfander, Hanspeter

, p. 1980 - 1985 (2007/10/02)

A novel synthesis of (-)-(R)-cembrene A ...

Synthesis of (-)-(R)-nephthenol and (-)-(R)-cembren A

Schwabe,Farkas,Pfander

, p. 292 - 297 (2007/10/02)

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31570-39-5 Process route

geranylgeranyl pyrophosphate
13100-78-2

geranylgeranyl pyrophosphate

(–)-(R)-cembrene A
38748-84-4,57918-06-6,71213-92-8,72690-72-3,72690-73-4,72691-72-6,73246-00-1,105662-19-9,139492-81-2,31570-39-5

(–)-(R)-cembrene A

(S,1E,5E,9E)-1,5,9-trimethyl-12-(prop-1-en-2-yl)cyclotetradeca-1,5,9-triene
72691-72-6

(S,1E,5E,9E)-1,5,9-trimethyl-12-(prop-1-en-2-yl)cyclotetradeca-1,5,9-triene

Conditions
Conditions Yield
With β-himachalene synthase elution fraction; In water; at 28 ℃; for 4h; Overall yield = 1.0 mg; Enzymatic reaction;
61 % ee
(3R,6E,10E)-6,10-dimethyl-3-isopropenylpentadeca-6,10-dien-1-al
79859-58-8

(3R,6E,10E)-6,10-dimethyl-3-isopropenylpentadeca-6,10-dien-1-al

(–)-(R)-cembrene A
38748-84-4,57918-06-6,71213-92-8,72690-72-3,72690-73-4,72691-72-6,73246-00-1,105662-19-9,139492-81-2,31570-39-5

(–)-(R)-cembrene A

Conditions
Conditions Yield
With titanium tetrachloride; zinc; In 1,2-dimethoxyethane; for 3h; Ambient temperature;
81%

31570-39-5 Upstream products

  • 53915-41-6
    53915-41-6

    2-[(1R,3E,7E,11E)-4,8,12-trimethylcyclotetradeca-3,7,11-trien-1-yl]propan-2-ol

  • 72690-76-7
    72690-76-7

    ((1R,2S,5R)-2-Isopropyl-5-methyl-cyclohexyloxy)-acetic acid (2E,6E,10E)-(1R,14S)-14-isopropenyl-3,7,11-trimethyl-cyclotetradeca-2,6,10-trienyl ester

  • 79897-31-7
    79897-31-7

    (1R,3S,4S,7E,11E)-3,4-epoxycembra-7,11,15-triene

  • 79859-58-8
    79859-58-8

    (3R,6E,10E)-6,10-dimethyl-3-isopropenylpentadeca-6,10-dien-1-al

31570-39-5 Downstream products

  • 37867-25-7
    37867-25-7

    2E,6E,10E-Cembratrien

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